WO2018015138A1 - Procédé de production d'acide sulfurique à partir de charges contenant du soufre avec trempe au gaz - Google Patents

Procédé de production d'acide sulfurique à partir de charges contenant du soufre avec trempe au gaz Download PDF

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Publication number
WO2018015138A1
WO2018015138A1 PCT/EP2017/066593 EP2017066593W WO2018015138A1 WO 2018015138 A1 WO2018015138 A1 WO 2018015138A1 EP 2017066593 W EP2017066593 W EP 2017066593W WO 2018015138 A1 WO2018015138 A1 WO 2018015138A1
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WIPO (PCT)
Prior art keywords
process gas
gas
temperature
sulfuric acid
stream
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Application number
PCT/EP2017/066593
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English (en)
Inventor
Morten Thellefsen
Martin MØLLERHØJ
Original Assignee
Haldor Topsøe A/S
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Filing date
Publication date
Application filed by Haldor Topsøe A/S filed Critical Haldor Topsøe A/S
Priority to US16/309,305 priority Critical patent/US10532930B2/en
Priority to RU2019104727A priority patent/RU2746896C2/ru
Priority to CN201780045046.7A priority patent/CN109476479A/zh
Publication of WO2018015138A1 publication Critical patent/WO2018015138A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00—Sulfur; Compounds thereof
    • C01B17/69—Sulfur trioxide; Sulfuric acid
    • C01B17/90—Separation; Purification
    • C01B17/92—Recovery from acid tar or the like, e.g. alkylation acids
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/14—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
    • B01D53/1456—Removing acid components
    • B01D53/1468—Removing hydrogen sulfide
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00—Sulfur; Compounds thereof
    • C01B17/48—Sulfur dioxide; Sulfurous acid
    • C01B17/50—Preparation of sulfur dioxide
    • C01B17/501—Preparation of sulfur dioxide by reduction of sulfur compounds
    • C01B17/503—Preparation of sulfur dioxide by reduction of sulfur compounds of sulfuric acid
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00—Sulfur; Compounds thereof
    • C01B17/48—Sulfur dioxide; Sulfurous acid
    • C01B17/50—Preparation of sulfur dioxide
    • C01B17/508—Preparation of sulfur dioxide by oxidation of sulfur compounds
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00—Sulfur; Compounds thereof
    • C01B17/69—Sulfur trioxide; Sulfuric acid
    • C01B17/74—Preparation
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/10—Process efficiency
    • Y02P20/129—Energy recovery, e.g. by cogeneration, H2recovery or pressure recovery turbines

Definitions

  • the present invention relates to a method for production of sulfuric acid from sulfur containing feeds with high potential for formation of so-called sticky dust that can plug conventional waste heat boilers, forcing unplanned shut downs of the entire sulfuric acid plant. More specifically, the invention relates to a method for the production of sulfur trioxide from a feed stream comprising sulfur-containing compounds and dissolved metals and alkali metals, said process comprising the following steps : incineration in the presence of an 0 2 -rich stream and optionally a support fuel, whereby the sulfur-containing com ⁇ pounds in the feed stream are converted to SO 2 and the dis ⁇ solved metals and alkali metals are converted into a partly solidified dust, mixing the hot process gas from the incinerator with a stream of colder gas in a mixing unit, such that the temperature of the combined stream is below the particle so- lidification temperature, cooling of the combined gas stream in one or two heat ex ⁇ changers, removing solid dust particles from the combined gas stream in a dust removal device, optionally adding hot
  • the sulfur containing feed could be spent sulfuric acid from an alkylation process, in which sulfuric acid is act ⁇ ing as catalyst for the production of alkylate - i.e. a fuel additive.
  • the sulfuric acid gets contaminated with water and acid soluble oils and, to some extent, also corrosion products from the plant equip ⁇ ment (Fe, Cr, Ni ions) and ingress of alkaline (Na, K) ions, e.g. from alkylate purifying equipment.
  • This acid is withdrawn from the alkylation process, regenerated to concentrated sulfuric acid in a separate sulfuric acid plant and returned to the alkylation process.
  • a sulfur containing feed is the products from a coke oven gas cleaning process, in which 3 ⁇ 4S and HCN present in the coke oven gas are absorbed into an aqueous alkaline solution and converted into elemental sulfur (S) and salts of SCN " , S2O 3 2" and S0 4 2 ⁇ .
  • S elemental sulfur
  • S elemental sulfur
  • salts of SCN " , S2O 3 2" and S0 4 2 ⁇ Usually the correspond ⁇ ing cation is NH 4 + or Na + , depending on how the alkalinity is controlled, e.g. by N3 ⁇ 4 or NaOH addition.
  • the trade names for such coke oven gas cleaning processes are e.g. HPF, PDS, Perox and Stretford. These products are of low quality and value and can be converted into concentrated sulfuric acid to increase the utilization and value of the sulfur compounds.
  • the method of the present invention differs from the above prior art in that it comprises a step of mixing the hot process gas from the incinerator with a stream of colder gas in a mixing unit, such that the temperature of the com ⁇ bined stream is below the particle solidification tempera ⁇ ture.
  • the method of the present invention provides an improved way of producing S O 3 from feed streams comprising sulfur-containing compounds and dissolved metals, where the metals are removed as solids after cooling.
  • Fig. 1 is a known process layout for converting a feed stream into concentrated sulfuric acid
  • Fig. 2 shows the sulfuric acid process with a new type of waste heat boiler to be used according to the invention
  • Figs. 3 to 6 show different alternative process layouts to be used according to the invention.
  • the commonly used process layout for converting sulfur-containing feeds into concentrated sulfuric acid is shown in Fig. 1.
  • the feed stream comprising sulfur com- pounds and dissolved metals and alkali metals 1 is fed into a furnace 3, operating at 900-1100°C.
  • the following reactions take place, depending on the exact com ⁇ position of the feed: H 2 S0 4 -> S0 2 + 0.5 0 2 + H 2 0
  • support fuel 2 can be CH 4 , C 2 H6 and other hydrocarbon based fuels, but also H 2 S, CO and H 2 are applicable.
  • support fuels can be CH 4 , C 2 H6 and other hydrocarbon based fuels, but also H 2 S, CO and H 2 are applicable.
  • an 0 2 -rich stream 36 is directed to the fur ⁇ nace. Most often atmospheric air is used, because hot air 29 is produced in the sulfuric acid condenser 23 in the sulfuric acid plant.
  • the process gas 4 leaving the furnace 3 is cooled to 450- 600°C in a waste heat boiler 5 in order to recover heat in the form of high pressure steam.
  • the steam pressure is in the range 20-85 bar gauge.
  • waste heat boiler for these appli- cations
  • fire tube boilers in which the process gas flows through a number of parallel horizontal tubes.
  • the gas velocity is high (usually 25-50 m/sec) to provide a high convective heat transfer coefficient for ef ⁇ ficient heat transfer to the cooling media on the shell side of the tubes.
  • the cooling media is usually high pres ⁇ sure water, and heat is absorbed by means of phase transfer (i.e. boiling) .
  • phase transfer i.e. boiling
  • This design is well known and widely used in the industry.
  • Another type of waste heat boiler is the so-called water tube boiler, in which the process gas flows on the shell side of the tubes and water/steam is flowing on the inside of the tubes. Water tube boilers also rely on convective heat transfer, and thus the gas velocity must be high and the distance between the tubes must be small.
  • the process gas 6 leaving the waste heat boiler is then further cooled to 375-450°C in a dilution air heater 10.
  • a steam superheater could be installed or the upstream waste heat boiler 5 could be designed to cool the process gas to 375-450°C.
  • dust is removed from the process gas in an electrostatic precipitator 13.
  • Other types of dust removal equipment can also be used, such as ceramic filters.
  • hot dilution air 45 is added to the process gas 14 in order to provide sufficient oxygen for the catalytic oxidation of SO 2 to SO 3 . This position for air addition ensures that the size of the furnace 3, the waste heat boiler 5, the dilution air heater 10 and the electrostatic precipitator 13 is minimized.
  • the diluted process gas 16 then enters the SO 2 converter 17 at 375-420°C.
  • the converter consists of a number of cata ⁇ lyst layers 18 with heat exchangers 19 installed between the catalyst layers.
  • the conversion of SO 2 to SO 3 is an ex ⁇ othermal reaction, and in order to maximize the overall SO 2 conversion it is normal practice to use a number of cata ⁇ lyst layers, each consecutive layer operating at a lower temperature, to ensure the highest conversion efficiency possible.
  • the number of catalyst layers is between 1 and 4, with 3 as the most common number for these applications.
  • the heat exchangers 19 between the catalyst layers are de ⁇ signed to provide the optimal process gas temperature at the inlet of each of the catalyst layers 18.
  • cooling me ⁇ dia usually saturated and/or superheated steam is used, but air, molten salt or hot pressurized water can be used too .
  • the converted process gas is cooled to 250-310°C in a boiler 20 before the pro- cess gas leaves the SO 2 converter 17.
  • the SO 3 starts to react with 3 ⁇ 40 in the gas phase to form H 2 SO 4 vapor.
  • the H 2 SO 4 product 24 is cooled to around 40°C and sent to battery limit for storage or direct use.
  • the H 2 SO 4 concen- tration is 93-98.5% w/w, depending on the H 2 O/SO 3 ratio in the process gas 22.
  • the cooling media 28 for the sulfuric acid condensation is atmospheric air, and the hot air 29 leaving the condenser can be recycled back to the front end of the sulfuric acid plant as pre-heated combustion air 36 and hot dilution air 44.
  • a hot air blower 32 is needed to recycle the hot air. Any hot air not used for these purposes 30 can be mixed with the cleaned gas 25 to provide a dry clean gas (and thus dry stack), or the heat can be utilized for e.g.
  • the so-called dry gas sulfuric acid technology has a dif ⁇ ferent layout.
  • the furnace and waste heat boiler are simi ⁇ lar to those used in the wet gas technology as described above and shown in Fig. 1, but after leaving the waste heat boiler, the process gas is quenched to 50-60°C to wash out dust and remove water from the process gas. The remaining water in the process gas is removed in a drying tower, us ⁇ ing concentrated sulfuric acid as the drying agent.
  • the cold dry S0 2 -containing process gas is then reheated, SO 2 is catalytically oxidized to SO 3 and the formed SO 3 is ab ⁇ sorbed into concentrated sulfuric acid in a dedicated ab ⁇ sorption tower.
  • Both the wet and dry processes are able to convert the above mentioned feeds, as long as the concentrations of the dust forming metals and alkali metals are sufficiently low. If the tolerance for these impurities is exceeded, both processes will suffer from the effect of dust formation and deposition.
  • the dissolved metals and alkali metals in the feed will form oxides and/or sulfates in either solid or liquid state.
  • the temperature and chemistry of the par- tides determine, to which extent the particles will be liquid.
  • These particles will be transported out of the fur ⁇ nace together with the process gas 4. It is well known in the industry that high concentrations of Na and K will re ⁇ sult in the formation of a 2 S0 4 /K 2 S0 4 compounds, which will be at least partly liquefied at the high furnace tempera ⁇ tures. When these "sticky" particles get into contact with the cold surfaces of the waste heat boiler 5, the particles will stick to the surface and quickly solidify to form a solid deposit layer.
  • the thickness of the deposit layer grows over time, and eventually the layer will become so thick that the process gas flow through the waste heat boiler tube (in a fire tube boiler) or between the waste heat boiler tubes (in a water tube boiler) is hampered to a degree where it is not possible to operate the plant, and so the plant has to be shut down for removal of these de ⁇ posits.
  • the operating time between such shut-downs can be more than a year for very clean feeds, but for feeds with very high concentrations of especially alkali metals, the tubes can plug after less than 24 hours of operation.
  • Radiation-type heat exchangers are also available, and they are plugging resistant as the distance from metal surface to metal surface is large and the heat transfer length for radiation is much longer than for convective heat transfer.
  • the radiation-type heat exchangers can either be of the gas/gas or the gas/steam type, of which the former is only used for small capacities whereas the latter is used for larger capacities, e.g. for power plant boilers.
  • This lay ⁇ out is also shown in Fig. 2 and, apart from the new type of waste heat boiler in position 5, the process gas layout is the same as the conventional layout as shown in Fig. 1.
  • the plugging tendency of the dust particles in the process gas depends on their "stickiness", i.e. they must be at least partly liquefied to become sticky. At temperatures below this liquidification/solidification temperature, the dust particles will solidify and become non-sticky. The so ⁇ lidification temperature depends on the chemical composi ⁇ tion of the particles and to some extent on the chemical composition of the surrounding process gas. As a rule of thumb, one can assume that the dust becomes non-sticky at a temperature below around 600°C, when the dust stickiness can be attributed to the presence of a 2 S0 4 and K 2 SO 4 in the dust particles.
  • the present invention describes a process in which the dust particles in the process gas are cooled from the high tem ⁇ perature at the outlet of the furnace to a temperature be- low the solidification temperature without being exposed to cold surfaces on which the particles can deposit, solidify and build up a deposit layer.
  • the process gas cooling is carried out by mixing the hot process gas from the furnace with a stream of colder gas, such that the temperature of the combined stream is below the particle solidification temperature. After the mixing, the process gas can be exposed to cold heat exchange sur ⁇ faces without risking any deposit layer build-up due to particle solidification.
  • the cold stream could e.g. be at ⁇ mospheric air, hot atmospheric air and/or recycled process gas .
  • the sulfur containing feed 1 is fed into the furnace 3, op- erating at around 1000°C. At this temperature, sulfur com ⁇ pounds and hydrocarbons as well as any NH 4 + salts are con ⁇ verted into SO2, CO2, H2O, 2 and small amounts of NO/NO2 and SO 3 . Most often the feed stream does not have a suffi ⁇ ciently high heating value to sustain the high temperature in the furnace, and thus support fuel 2 is needed.
  • Oxygen for the combustion processes is supplied via line 36, which is preheated air from the sulfuric acid condenser 23 and combustion air heater 35.
  • the combustion air heater 35 is optional, but has the advantage of reducing the support fuel consumption.
  • the combustion air leaving the sulfuric acid condenser 23 has a temperature of 200-260°C and can be heated up to 450°C in the combustion air heater 35.
  • the process gas leaving the furnace 3 is exactly as de ⁇ scribed for the conventional layout.
  • the hot process gas is then mixed with cold atmospheric air 38, which has been pressurized in a cold air blower 39 before admitted via line 40 to the mixing chamber 8.
  • cold air blower 39 There are numerous ways of mixing these two streams, e.g. adding the cold air via a number of nozzles located in a "ring" arrangement, covering the periphery of the mixing chamber or blowing in the air via a number of nozzles in a tangential arrangement, such that the cold air makes a swirl around the hot process gas.
  • Static mixers could also be installed downstream the mixing point, but care should be taken to ensure that the surfaces of the mixer material are not below the solidification tem- perature of the dust particles. Otherwise the surfaces of the mixer should be kept separated from the dust laden pro ⁇ cess gas.
  • the mixing chamber could be as simple as a brick lined chamber, just extending the brick lined furnace chamber 3.
  • the well-mixed process gas 9 leaving the mixing chamber 8 is around 450-500°C, and thus the dust particles are non- sticky.
  • the process gas 9 is then cooled to 400-450°C in a heat exchanger 10, which can be a waste heat boiler (water tube or fire tube) or the combustion air preheater 35.
  • the cooled process gas then enters the electrostatic pre ⁇ cipitator 13, in which the dust is separated from the pro ⁇ cess gas and withdrawn from the bottom of the precipitator.
  • the cleaned process gas 14 then enters the SO 2 converter 17.
  • the following SO 2 conversion and sulfuric acid conden- sation is exactly as described in the conventional layout.
  • This simple process gas layout has a high resistance against fouling as only a single heat exchanger is in contact with the dust laden process gas, i.e. the availability of the plant is very high.
  • the drawback of the layout is that the process gas flow through the process gas cooler 10 and electrostatic precip ⁇ itator 13 is high, and thus the equipment size and cost will increase.
  • Another drawback is that there is a small risk of sulfuric acid condensation in the mixing zone as it is possible to imagine that there can be surfaces in contact with the cold air (at say 20-60°C) that also can get into contact with the process gas containing a little SO 3 , which can condense as sulfuric acid at temperatures below roughly 200°C. A proper design of the gas/air mixing chamber will eliminate this risk.
  • FIG. 4 Another process layout is shown in Fig. 4.
  • the quench air 37 is hot air 29 from the sulfuric acid condensation tower 17.
  • the hot air is pressurized in a combustion air blower 32.
  • the requirements for O 2 for the SO 2 oxidation in the converter 17 is fulfilled with a temperature when leaving the mixing chamber 8 of 600°C, i.e. the hot air temperature corresponds very well to the O 2 demand re ⁇ quired.
  • the quench air 40 was "too cold" to en ⁇ sure the 600 °C mixing temperature when taking the O 2 demand into account, and the resulting process gas temperature was 450-500 °C.
  • the re ⁇ quired air flow for cooling would be much higher than the demand for O 2 in the converter 17, and the downstream plant would have to be designed for a higher process gas flow.
  • the optimum trade-off between O 2 demand and cooling re- quirements will depend on the composition of the feed 1 to the furnace 3 and the operation of the furnace.
  • FIG. 4 In the layout shown in Fig. 4, more heat has to be removed in the process gas cooler 10, which could be one single heat exchanger or two or more heat exchangers in series.
  • An example could be the combustion air heater 35 combined with a waste heat boiler to control the temperature of the pro ⁇ cess gas entering the electrostatic precipitator 13.
  • This layout is just as simple as that shown in Fig. 3. The ad- vantage is a better heat recovery, and the design of the mixing chamber becomes simpler, because all parts of the mixer will have a temperature above the sulfuric acid dew point temperature.
  • a third layout is shown in Fig. 5, in which the quenching stream 54 is process gas recycled from a position downstream the electrostatic precipitator 13.
  • a fraction of the process gas 14 leaving the precipitator 13 is directed to a heat exchanger 51 to cool the process gas from 400-450°C to 200-300°C.
  • a simple and energy effi- cient method consists in installing a boiler that uses the high pressure steam system used at other locations of the sulfuric acid plant, e.g. process gas cooler 20 and
  • the cooled quench gas 52 is then pressurized in quench gas blower 53 and sent to the mixing chamber 8 via line 54.
  • This dilution air is hot air 29 from the sulfuric acid condenser 24, which has been pressurized in com- bustion air blower 32 and further heated to 350-400°C in the dilution air heater 42.
  • the dilution air heater will typically be located in position 10 in order to optimize heat recovery.
  • the advantage of this layout is a slightly better heat re ⁇ covery than in the layout with hot air quench, cf. Fig. 4.
  • the quench gas cooler 51 and quench gas blower 53 are installed in a dust free process gas, thus minimizing the risk of fouling of the heat exchanger and blower.
  • the pro- cess gas flow through the plant is unchanged.
  • Another advantage is that the dilution air addition via line 45 reduces the dust concentration in the process gas 16 entering the SO 2 converter 17, which will reduce the plugging of the catalyst layers (especially 18a) due to capture of residual dust in the process gas 14 leaving the electrostatic precipitator 13.
  • the catalyst for converting SO 2 to SO 3 is very efficient in capturing dust particles and thus over time they plug due to the filling up of the volumes between the catalyst pellets with the dust.
  • this dust concentration at the inlet to the SO 2 converter 17 is equal to the conventional layout, cf. Fig. 1, whereas the layouts in Figs. 3 and 4 have a higher dust concentration at the inlet to the SO 2 converter.
  • the SO 2 converter can be designed with "sacrificial" catalyst layers, which can be bypassed when plugged with dust .
  • a fourth layout is shown in Fig. 6.
  • the layout resembles the layout in Fig. 5, but the process gas to be recycled for process gas quenching 64 is withdrawn at a position upstream from the electrostatic precipitator 13.
  • the dust laden process gas 60 is cooled in quench gas cooler 61 and pressurized in quench gas blower 63 before being fed to the mixing chamber 8 via line 64.
  • This layout has the advantage that the process gas flow through the electrostatic precip ⁇ itator is minimized, i.e. the flow through the precipitator is equal to that in the conventional layout as shown in Fig. 1. This saves on cost of the precipitator.
  • the quench gas cooler 61 and quench gas blower 63 both have to be de- signed for dust in the process gas, making them a little more expensive. Apart from these differences the total process gas flow and heat recovery is equal to the layout as in Fig. 5.
  • the calculations are carried out for a sulfuric acid plant, regenerating 100 metric tons/day of spent sulfuric acid from an alkylation process.
  • the furnace temperature is 1000°C, and the combustion air is preheated to 400°C in every layout. It is assumed that the dust concentration in the process gas leaving the electrostatic precipitator is 2 mg/Nm 3 , a value that is independent of the dust concentration at the inlet of the precipitator. Combustion air flow and fuel gas flow are equal for each layout .
  • the main results are shown in the table below.
  • the table compares five different process layouts for converting 100 metric ton/day of spent sulfuric acid into concentrated sulfuric acid.
  • the process layouts only differ from the outlet of the furnace to the inlet of the SO 2 converter. It is seen that in many ways the conventional layout is the preferred layout, as much of the equipment has the lowest flow and thus has the potential for lower cost too. This is evident for the electrostatic precipitator, but not neces ⁇ sarily evident for the heat exchangers as the different layouts provide possibilities for different heat exchanger layouts and materials of construction.
  • the quench solution To be able to operate without plugging of the waste heat boiler, the quench solution must be applied, but the pro ⁇ longed operation time comes at a potentially higher cost and/or a lower heat efficiency of the plant.
  • the heat exchange duty is defined as the heat transfer from one media to another in a position between the outlet of the furnace to the inlet of the SO 2 con ⁇ verter, i.e. waste heat boiler, quench gas cooler, combustion air heater and dilution air heater.
  • the heat exchang- ers in the rest of the plant are similar and not included in the comparison.
  • the steam export duty is defined as the heat transferred to the high pressure steam system in the entire sulfuric acid plant and is thus a measure of the heat recovery efficiency of the plant layouts.
  • the heat recovery can be higher if e.g. the hot air from the sulfuric acid condenser, not used for combustion/quench/dilution air, can be utilized for e.g. low pressure steam production, drying purposes and district heating.
  • the cold air quench layout is very simple with the lowest heat exchange surface installed between the furnace and SO 2 converter. This is at the cost of steam export duty, but for a small plant with little use of steam, this layout could be the best solution.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treating Waste Gases (AREA)
  • Exhaust Gas Treatment By Means Of Catalyst (AREA)
  • Waste-Gas Treatment And Other Accessory Devices For Furnaces (AREA)
  • Electrostatic Separation (AREA)
  • Air Supply (AREA)

Abstract

L'invention concerne une installation pour la production de trioxide de souffre à partir d'un flux d'alimentation contenant des composés contenant du souffre et des metaux dissous et des métaux alcalins, par un procédé qui implique une trempe de gaz, qui comprend un four d'incinération, un dispositif de mélange et/ou de chauffage de l'air de dilution, un dispositif de dépoussiérage et un convertisseur de SO2. L'installation peut en outre comprendre un condenseur destiné à produire de l'acide sulfurique.
PCT/EP2017/066593 2016-07-21 2017-07-04 Procédé de production d'acide sulfurique à partir de charges contenant du soufre avec trempe au gaz WO2018015138A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US16/309,305 US10532930B2 (en) 2016-07-21 2017-07-04 Method for production of sulfuric acid from sulfur containing feeds with gas quenching
RU2019104727A RU2746896C2 (ru) 2016-07-21 2017-07-04 Способ получения серной кислоты из серосодержащего исходного сырья с быстрым газовым охлаждением
CN201780045046.7A CN109476479A (zh) 2016-07-21 2017-07-04 采用气体骤冷从含硫进料生产硫酸的方法

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DKPA201600440 2016-07-21
DKPA201600440 2016-07-21

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WO2018015138A1 true WO2018015138A1 (fr) 2018-01-25

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WO (1) WO2018015138A1 (fr)

Cited By (1)

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TWI704013B (zh) * 2018-04-23 2020-09-11 日商三菱日立電力系統股份有限公司 熱交換器

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CN114307868A (zh) * 2020-10-12 2022-04-12 南京华电节能环保股份有限公司 一种接触法硫酸工艺用多级转化塔

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EP2942323A1 (fr) 2014-05-09 2015-11-11 Haldor Topsøe A/S Production d'acide sulfurique à partir de produit de désulfuration de gaz de four à coke

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US20190308879A1 (en) 2019-10-10
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US10532930B2 (en) 2020-01-14
CN109476479A (zh) 2019-03-15

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